Top 6 Clinical research coordinator Jobs in Cortland Ny

Clinical Research Associate, IQVIA Biotech
IQVIA —Ithaca, NY
- $71,900 - $169,300 a year
- Full-time
- Bachelor's degree
- Travel
- Experience equivalent to degree accepted
Clinical Research Regulatory Coordinator
Smith Allergy and Asthma —Cortland, NY
- $22 - $30 an hour
- Full-time
- Mid-level
- Continuous improvement
- In-person
Quick Apply
Per Diem Clinical Research Nurse - Home Visits
Science 37 —Ithaca, NY
- $50 - $55 an hour
- Nights as needed
- Nursing
- RN License
- BLS Certification
4d
Clinical Research Coordinator
Cornell University —Ithaca, NY
- $65,447 - $75,632 a year
- Weekends as needed
- Mid-level
- Master's degree
- University
- Adoption assistance
- Parental leave
Coordinator, Research Development & Strategic Initiatives
Cornell University —Ithaca, NY
- $30.02 - $34.88 an hour
- Online Application
- Hybrid work
- Microsoft Outlook
- Research
- Mid-level
- Health insurance
- Tuition reimbursement
Clinical Donation Coordinator I - PeeDee Region
WE ARE SHARING HOPE SC —United States
- On call
- Mid-level
- Operating room
- 2 years

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Clinical Research Associate, IQVIA Biotech
IQVIA —Ithaca, NY
Bachelor’s degree in life sciences or health-related field (or equivalent experience). Monitor study progress by tracking regulatory submissions, subject…
$71,900 - $169,300 a year
CRA 1, IQVIA Biotech
IQVIA —Ithaca, NY
During these visits, you will review essential documents, assess protocol adherence, oversee data entry and query resolution, and ensure maintenance of both the…
$71,900 - $145,300 a year

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Clinical Research Coordinator
OhioHealth —Columbus, OH
This position performs basic day to day activities related to clinical research studies including recruit and screen participants, obtains informed consent,…
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The Ohio State University Wexner Medical Center —Columbus, OH
Bachelor’s Degree in Biological Sciences, Health Sciences or medical field, or equivalent combination of education experience required.
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Clinical Research Associate, IQVIA Biotech

IQVIA -
Ithaca, NY

Apply Now

Job Details

Full-time
$71,900 - $169,300 a year

Qualifications

Regulatory compliance
ICH guidelines
Clinical quality assurance standards
Oncology

Full Job Description

Ithaca, United States of America | Full time | Field-based | R1520467

IQVIA Biotech is now hiring for CRA 2 with a minimum of 1 year of on-site monitoring and will also consider CRA 1 candidates with a minimum of 6 months on-site monitoring experience. Must have experience monitoring in oncology solid tumor.

IQVIA Biotech is a full-service CRO purpose-built to serve biotech sponsors. With over 25 years of experience, we offer agile, therapeutically aligned solutions and trusted partnerships that help bring breakthrough treatments to patients faster.

Job Overview
We are seeking a dedicated Clinical Research Associate (CRA) to join our team and play a key role in ensuring the successful execution of clinical trials. In this position, you will be responsible for monitoring and managing clinical sites to ensure compliance with study protocols, regulatory requirements, and sponsor expectations. Your work will directly contribute to the integrity and quality of clinical research data.

Key Responsibilities

Conduct all types of site visits—selection, initiation, monitoring, and close-out in alignment with the contracted scope of work, Good Clinical Practice (GCP), and ICH guidelines.
Collaborate with site staff to implement and track subject recruitment strategies that align with project timelines and enrollment goals.
Deliver protocol and study-specific training to site personnel and maintain consistent communication to manage expectations and resolve issues.
Assess site performance and adherence to the protocol, escalating quality concerns as needed to ensure compliance and data integrity.
Monitor study progress by tracking regulatory submissions, subject enrollment, case report form (CRF) completion, and resolution of data queries.
Ensure that essential documents are collected and maintained in both the Trial Master File (TMF) and the Investigator Site File (ISF) in accordance with regulatory standards.
Document site management activities, visit outcomes, and follow-up actions through detailed reports and correspondence.
Work closely with cross-functional project teams to support study execution and ensure alignment with project goals.
Depending on the project, you may also support site-level recruitment planning and financial management, including invoice collection and budget tracking.

Qualifications

Bachelor’s degree in life sciences or health-related field (or equivalent experience).
Requires at least 1 year of on-site monitoring experience.
Strong understanding of GCP, ICH guidelines, and regulatory requirements.
Ability to travel as required by the project.

IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com

IQVIA is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, status as a protected veteran, or any other status protected by applicable law. https://jobs.iqvia.com/eoe

IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

The potential base pay range for this role, when annualized, is $71,900.00 - $169,300.00. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits.

Where you'll work

Field-based

You’ll work where the action is — out in the field, directly engaging with our customers, sites or partners. Field-based roles offer the opportunity to build relationships face-to-face, gain real-world insights and make a tangible impact.

Culture

Culture at IQVIA is built on a shared belief: that when people are empowered with better data, smarter technology and deeper expertise, they can change what’s possible for patients. Across every team and every corner of the globe, you’ll find colleagues who genuinely care — about the mission and about each other. That’s what makes this a place where people tend to stay, grow and do the best work of their careers.

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Refine Your Search

clinical research coordinator jobs in cortland ny

Clinical Research Associate, IQVIA Biotech

Clinical Research Regulatory Coordinator

Per Diem Clinical Research Nurse - Home Visits

Clinical Research Coordinator

Coordinator, Research Development & Strategic Initiatives

Clinical Donation Coordinator I - PeeDee Region

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